[한국화이자제약] Medical Research Associate (1yr contract)

[인사팀]

[한국화이자제약] Medical Research Associate (1yr contract)

Key Responsibilities

[1] IIR & PSR Coordination

• Manages the whole operational process of IIR and PSR.

• Proactively communicates with the investigators regarding the operational aspects of IIR/PSR.

• Arranges local review committee (LRC), drafts meeting minutes, sends approval or declination letter to investigator and archives the documents in the system.

• In review process, keeps constant contact with the global IIR Manager.

• Once the IIR proposal is forwarded to the GRC(Grant Review Committee), attends the GRC in collaboration with MM

• After the approval of IIR, if needed, oversights the whole study drug order and delivery process

• Manages contract processing including preparing FCPA documents, drafting contracts, communicating with site’s contract reviewers

• Requests payment based on the payment schedule in the contracts and keep the records

• Periodically sends out the study status update form to the investigators to check thestatus of the study ; updates regularly to the global IIR Management System

• When the publication/amendment is locally reviewed by MM, supports the documentation using the standard template

• Tracks local IIR budget status by product and plans the budget estimation.

• Confirm‎s the submission status for PSR and tracks the global review progress in the system after local review and checks the receipt status of raw material by sites.

• Submits the IIR/PSR in the KRPIA online reporting system according to KRPIA clinical activity guidelines

[2] PMS management

• Responsible for developing PMS protocol, CRF & data privacy statement in consultation with medical manager.

• Responsible for delivering potential study sites to CRO in consultation with medical manager

• Communication with alliance partner and subcontracted CRO regarding overall PMS operations

• Checks the important PMS milestones and reports the progress & issues to medical manager & MAD

Requirements

- Bachelor Degree in pharmacy, nursing or biology

- Understanding on scientific and medical publications

- Experience as Clinical Research Associate is preferred

- English communication both in written and spoken formats

- Skills in documentation and archiving

- Required Pharmacist license

- Experienced in medical communication and clinical research in pharmaceutical industry at least 1 year

제출서류:

국/영문 이력서 및 자기소개서, Pfizer 개인정보 처리에 관한 동의서 (입사지원자용) (각종 증빙서류는 서류전형합격자에 한해 추후제출)

접수방법:

 
- 지원 사이트: http://pfizercareers.com/apply 를 통해 접수.

화면 상단에 Apply -> Apply Now 클릭 -> Korea, Republic of 선택-> Job ID 984063 검색 -> 고유 계정 등록 -> 필수정보 입력 / 지원서, 개인정보 처리에 관한 동의서 파일 업로드 (MS Word/ PDF) -> 접수 완료)

- 국/영문 이력서와 자기소개서를 반드시 하나의 MS Word 파일로 제출해 주시고, 파일명은 영문으로 ‘지원자성명_지원포지션명’ (예, ‘GilDong Hong_MSR)로 명시한 후 ‘Resume’란에 업로드 해주시기 바랍니다.

- 또한, 개인정보 보호법의 요구사항에 따라, 첨부의 ‘개인정보 처리에 관한 동의서(입사지원자용)’에 동의 여부를 체크하신 후 지원 시 ‘Cover letter’란에 업로드 해주시기 바랍니다. 이는 법적 요구사항으로, 본 동의서가 첨부되지 않은 지원서류는 검토 대상에서 제외됩니다.

※ Pfizer 채용사이트(http://pfizercareers.com/apply)을 통한 지원 이외의 이메일 및 우편접수 등은 받지 않습니다.

서류마감기한: 7월 19일 (금) 오후 3:00까지

[입사지원서 다운로드]

개인정보처리동의서(입사지원자용).doc